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MicroBlate Fine

FDA UDI

Class II (US FDA UDI)

by Creo Medical, Ltd.

Identity

Trade Name
MicroBlate Fine FDA UDI
Generic Name
Microwave ablation system probe, non-powered FDA UDI
Device Name
MicroBlate Fine (NP1) is a single-use, sterile electrosurgical instrument for use with the Creo Medical Electrosurgical system. It enables ablation of potential malignant lesions such as nodules or tumors. MicroBlate Fine, when used with the Creo Medical Electrosurgical System, is intended for use in coagulation (ablation) of soft tissue. FDA UDI
Model / Reference
7-NP1-100 FDA UDI
Description
MicroBlate Fine (NP1) is a single-use, sterile electrosurgical instrument for use with the Creo Medical Electrosurgical system. It enables ablation of potential malignant lesions such as nodules or tumors. MicroBlate Fine, when used with the Creo Medical Electrosurgical System, is intended for use in coagulation (ablation) of soft tissue. FDA UDI

Identifiers

Catalog Number
7-NP1-100 FDA UDI
Primary DI / UDI-DI
05060359560971 FDA UDI
510(k) Number
K221672 FDA UDI
FDA Product Code
NEY FDA UDI
GMDN Term
Microwave ablation system probe, non-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Length — 1.9 Meter FDA UDI
Outer Diameter — 2.4 Millimeter FDA UDI

Category: Microwave ablation system probe, non-powered

MicroBlate Fine by Creo Medical, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microwave ablation system probe, non-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Creo Medical, Ltd.

Sources (1)

  • FDA UDI 72028893-3081-49e9-987d-e84c36a8e8ba 38 fields · synced May 30, 2026